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Acebutolol Hydrochloride

NDC 53746-669 · Amneal Pharmaceuticals of New York LLC

Generic nameAcebutolol Hydrochloride
Dosage formCAPSULE
RouteORAL
Active ingredient(s)ACEBUTOLOL HYDROCHLORIDE
Strength200 mg/1
Pharmacologic classAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
Marketing categoryANDA

Packages

53746-669-01 — 100 CAPSULE in 1 BOTTLE (53746-669-01)

53746-669-05 — 500 CAPSULE in 1 BOTTLE (53746-669-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42291-010 — Acebutolol Hydrochloride, 50268-050 — Acebutolol Hydrochloride, 51407-666 — Acebutolol Hydrochloride, 51407-667 — Acebutolol Hydrochloride, 53746-670 — Acebutolol Hydrochloride, 62559-255 — Acebutolol Hydrochloride, 62559-256 — Acebutolol Hydrochloride, 65162-669 — Acebutolol Hydrochloride, 65162-670 — Acebutolol Hydrochloride

Poisoning, adverse-effect and underdosing codes for this drug

The ICD-10-CM Table of Drugs and Chemicals carries these diagnosis codes for this drug — a drug-name match derived from FDA's product name and the Table of Drugs and Chemicals, not a CMS-published pairing.

T44.7X1 — Poisoning by beta-adrenoreceptor antagonists, accidental (unintentional), T44.7X2 — Poisoning by beta-adrenoreceptor antagonists, intentional self-harm, T44.7X3 — Poisoning by beta-adrenoreceptor antagonists, assault, T44.7X4 — Poisoning by beta-adrenoreceptor antagonists, undetermined, T44.7X5 — Adverse effect of beta-adrenoreceptor antagonists, T44.7X6 — Underdosing of beta-adrenoreceptor antagonists

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.